Canonical Allele Identifier: CA357056931
Gene: GNRHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754328T>A , CM000666.2:g.67754328T>A GRCh38
NC_000004.11:g.68620046T>A , CM000666.1:g.68620046T>A GRCh37
NC_000004.10:g.68302641T>A NCBI36
NG_009293.1:g.6759A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.8A>T MANE Select ENSP00000226413.5:p.Asn3Ile
ENST00000226413.4:c.8A>T ENSP00000226413.4:p.Asn3Ile
ENST00000420975.2:c.8A>T ENSP00000397561.2:p.Asn3Ile
NM_000406.2:c.8A>T NP_000397.1:p.Asn3Ile
NM_001012763.1:c.8A>T NP_001012781.1:p.Asn3Ile
NM_000406.3:c.8A>T MANE Select NP_000397.1:p.Asn3Ile
NM_001012763.2:c.8A>T NP_001012781.1:p.Asn3Ile